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Atomfair 3-Chloro-4-fluorophenol C6H4ClFO

Description 3-Chloro-4-fluorophenol (CAS No. 2613-23-2) is a high-purity halogenated phenol derivative with the molecular formula C6H4ClFO . This compound is a versatile intermediate in organic synthesis, characterized by its distinct chloro and fluoro substituents on the phenolic ring, which enhance its reactivity and utility in cross-coupling reactions, pharmaceutical synthesis, and agrochemical applications. With a purity grade of ??98%, our product is rigorously tested via GC/MS, HPLC, and NMR to ensure consistency and reliability for research and industrial use. Suitable for use under inert conditions due to its sensitivity to oxidation, it is supplied in amber glass vials or bulk packaging…

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Description

Description

3-Chloro-4-fluorophenol (CAS No. 2613-23-2) is a high-purity halogenated phenol derivative with the molecular formula C6H4ClFO. This compound is a versatile intermediate in organic synthesis, characterized by its distinct chloro and fluoro substituents on the phenolic ring, which enhance its reactivity and utility in cross-coupling reactions, pharmaceutical synthesis, and agrochemical applications. With a purity grade of ??98%, our product is rigorously tested via GC/MS, HPLC, and NMR to ensure consistency and reliability for research and industrial use. Suitable for use under inert conditions due to its sensitivity to oxidation, it is supplied in amber glass vials or bulk packaging with optional argon sealing for extended shelf life. Ideal for researchers developing advanced materials, APIs, or specialty chemicals.

  • CAS No: 2613-23-2
  • Molecular Formula: C6H4ClFO
  • Molecular Weight: 146.54
  • Exact Mass: 145.9934706
  • Monoisotopic Mass: 145.9934706
  • IUPAC Name: 3-chloro-4-fluorophenol
  • SMILES: C1=CC(=C(C=C1O)Cl)F
  • Synonyms: 3-Chloro-4-fluorophenol, 2613-23-2, EINECS 220-042-5, DTXSID70180762, DTXCID10103253

Application

3-Chloro-4-fluorophenol serves as a key building block in the synthesis of pharmaceuticals, particularly in the development of antimicrobial and anti-inflammatory agents. Its halogenated structure makes it valuable for Suzuki-Miyaura and Buchwald-Hartwig coupling reactions in drug discovery. The compound is also employed in agrochemical research for creating herbicides and pesticides with enhanced activity. Additionally, it finds use in material science as a precursor for functionalized polymers and liquid crystals.

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